Development Level

Tbio 1 | 11,445

Disease

Abnormality of vision 1 | 40
Accessory rib 1 | 10
Alveolar rhabdomyosarcoma 1 | 7
Aplasia/Hypoplasia involving the nose 1 | 5
Atelectasis 1 | 8
Atresia of nasolacrimal duct 1 | 4
Atresia of vagina 1 | 10
Autosomal dominant contiguous gene syndrome 1 | 2
Blonde eyebrow 1 | 5
Brachydactyly 1 | 156
Bushy eyebrows 1 | 49
Carpal synostosis 1 | 12
Class III malocclusion 1 | 78
Cleft palate with cleft lip 1 | 23
Congenital Hand Deformities 1 | 8
Congenital deafness 1 | 185
Congenital diaphragmatic hernia 1 | 67
Congenital hypoplasia of nose 1 | 5
Congenital neurologic anomalies 1 | 20
Congenital sensorineural hearing loss 1 | 12
Convex nasal bridge 1 | 57
Craniofacial Abnormalities 1 | 151
Craniofacial deafness hand syndrome 1 | 1
Cutaneous finger syndactyly 1 | 11
Deafness 1 | 198
Decreased projection of maxilla 1 | 66
Deficiency of upper jaw bones 1 | 66
Downward slant of palpebral fissure 1 | 158
Ectomesenchymoma 1 | 5
Ewing sarcoma 1 | 25
Flat face 1 | 52
Grey eyebrow 1 | 5
Grey eyelashes 1 | 5
Hand Deformities, Congenital 1 | 8
Hearing Loss, Partial 1 | 185
Heterochromia iridis 1 | 9
Hirschsprung Disease 1 | 31
Hirschsprung's disease 1 | 46
Hypertrophy of lower jaw 1 | 78
Hypoplasia of the maxilla 1 | 66
Hypoplastic iris stoma 1 | 4
Hypotrophic malar bone 1 | 129
Hypotrophic maxilla 1 | 66
Hypotrophic nose 1 | 5
Increased size of mandible 1 | 78
Inverted V-shaped upper lip 1 | 19
Joint stiffness 1 | 84
Klein's Syndrome 1 | 1
Lacrimation abnormality 1 | 4
Malar flattening 1 | 129
Mandibular hyperplasia 1 | 78
Maxillary retrognathia 1 | 66
Megacolon 1 | 29
Microphthalmia 1 | 76
Narrow face 1 | 54
Narrow nose 1 | 20
Nervous System Malformations 1 | 10
Neural Tube Defects 1 | 31
Oral cleft 1 | 18
Piebaldism 1 | 15
Pinched bridge of nose 1 | 14
Pinched nasal bridge 1 | 14
Premature canities 1 | 24
Prominent nasal bridge 1 | 57
Retinal depigmentation 1 | 12
Retrusion of upper jaw bones 1 | 66
Rhabdomyosarcoma 1 | 39
Rhabdomyosarcoma, Alveolar 1 | 4
Sarcoma 1 | 62
Scapular weakness 1 | 23
Sensorineural hearing loss 1 | 106
Sinonasal undifferentiated carcinoma 1 | 2
Spinal Dysraphism 1 | 12
Sprengel deformity 1 | 16
Supernumerary vertebra 1 | 2
Synophrys 1 | 40
Synostosis of carpal bones 1 | 9
Synovial sarcoma 1 | 25
Tented mouth 1 | 19
Tented upper lip 1 | 19
Thin face 1 | 54
Thin hypoplastic alae nasi 1 | 51
Tietz syndrome 1 | 6
Ulnar deviation of the wrist 1 | 8
Vagina absent 1 | 2
Vagina aplasia 1 | 2
Waardenburg Syndrome 1 | 1
Waardenburg Syndrome Type 1 1 | 1
Waardenburg Syndrome, Type 1 1 | 1
Waardenburg syndrome type 3 1 | 1
Waardenburg's syndrome 1 | 17
White eyebrows 1 | 5
White eyelashes 1 | 5
White forelock 1 | 12
White hair 1 | 7
Winged scapula 1 | 23
blue iris (physical finding) 1 | 17
hearing impairment 1 | 199
hypopigmented skin patch 1 | 59
mandibular excess (physical finding) 1 | 78

Tissue

Blood and immune system 1 | 16,909
Cardiovascular System 1 | 15,192
Digestive Tract 1 | 17,369
Endocrine System 1 | 18,159
Female tissues 1 | 17,400
Liver and Pancreas 1 | 16,750
Male tissues 1 | 17,142
Nervous System 1 | 16,725
Respiratory system 1 | 16,393
Skin and soft tissues 1 | 17,230
Urinary Tract 1 | 16,678

Target Family

Transcription Factor 1 | 1,400

OMIM Phenotype

Craniofacial-deafness-hand syn... 1 | 1
Abacavir hypersensitivity, sus... 35 | 35
Phenotype: {Spondyloarthropath... 35 | 35
Stevens-Johnson syndrome, susc... 35 | 35
Synovitis, chronic, susceptibi... 35 | 35
Toxic epidermal necrolysis, su... 35 | 35
Phenotype: {Hypersensitivity s... 21 | 21
HIV-1 viremia, susceptibility ... 14 | 14
Phenotype: {Psoriasis suscepti... 14 | 14
Multiple sclerosis, susceptibi... 13 | 13
Phenotype: {Sarcoidosis, susce... 13 | 13
Colorectal cancer, somatic 8 | 8
Gastric cancer, somatic 6 | 6
Diabetes mellitus, noninsulin-... 5 | 5
Pheochromocytoma 5 | 5
ACTH-independent macronodular ... 4 | 4
Alzheimer disease, susceptibil... 4 | 4
Malaria, resistance to 4 | 4
McCune-Albright syndrome, soma... 4 | 4
Mycobacterium tuberculosis, su... 4 | 4
Osseous heteroplasia, progress... 4 | 4
Phenotype: Colorectal cancer, ... 4 | 4
Phenotype: Pseudohypoparathyro... 4 | 4
Phenotype: [Blood group 4 | 4
Phenotype: {Myocardial infarct... 4 | 4
Phenotype: {Schizophrenia, sus... 4 | 4
Pituitary adenoma 3, multiple ... 4 | 4
Pseudohypoparathyroidism Ib 4 | 4
Pseudohypoparathyroidism Ic 4 | 4
Pseudopseudohypoparathyroidism 4 | 4
Renal tubular dysgenesis 4 | 4
Tetralogy of Fallot 4 | 4
Afibrinogenemia, congenital 3 | 3
Aplastic anemia 3 | 3
Bladder cancer, somatic 3 | 3
COACH syndrome 3 | 3
Central hypoventilation syndro... 3 | 3
Dejerine-Sottas disease 3 | 3
Diabetes mellitus, permanent n... 3 | 3
LADD syndrome 3 | 3
Leukemia, acute myeloid 3 | 3
Lung cancer, susceptibility to 3 | 3
Mismatch repair cancer syndrom... 3 | 3
Multiple pterygium syndrome, l... 3 | 3
Myocardial infarction, suscept... 3 | 3
Neuropathy, distal hereditary ... 3 | 3
Omenn syndrome 3 | 3
Paraganglioma and gastric stro... 3 | 3
Parkinson disease, susceptibil... 3 | 3
Phenotype: Anterior segment dy... 3 | 3
Phenotype: Bethlem myopathy 1 3 | 3
Phenotype: Dysfibrinogenemia, ... 3 | 3
Phenotype: Epilepsy, progressi... 3 | 3
Phenotype: Leigh syndrome due ... 3 | 3
Phenotype: Orthostatic intoler... 3 | 3
Phenotype: {Breast cancer, sus... 3 | 3
Prostate cancer, susceptibilit... 3 | 3
Retinitis punctata albescens 3 | 3
Roussy-Levy syndrome 3 | 3
Schimmelpenning-Feuerstein-Mim... 3 | 3
Schizencephaly 3 | 3
Ullrich congenital muscular dy... 3 | 3
Arthrogryposis, distal, type 2... 2 | 2
Asthma, susceptibility to 2 | 2
Brachydactyly, type A2 2 | 2
Cerebrooculofacioskeletal synd... 2 | 2
De Sanctis-Cacchione syndrome 2 | 2
Epidermolysis bullosa simplex,... 2 | 2
Epidermolysis bullosa simplex,... 2 | 2
Epidermolysis bullosa simplex,... 2 | 2
Hypercholesterolemia, familial... 2 | 2
Hypofibrinogenemia, congenital 2 | 2
Ichthyosis, cyclic, with epide... 2 | 2
Jackson-Weiss syndrome 2 | 2
Leukemia, acute lymphoblastic,... 2 | 2
Leukemia, acute myeloid, somat... 2 | 2
Macular degeneration, age-rela... 2 | 2
Melanoma, cutaneous malignant,... 2 | 2
Microvascular complications of... 2 | 2
Ovarian cancer, somatic 2 | 2
Phenotype: Cockayne syndrome, ... 2 | 2
Phenotype: Epidermodysplasia v... 2 | 2
Phenotype: Epidermolysis bullo... 2 | 2
Phenotype: Epidermolytic hyper... 2 | 2
Phenotype: Hemochromatosis 2 | 2
Phenotype: Lacticacidemia due ... 2 | 2
Phenotype: Meesmann corneal dy... 2 | 2
Phenotype: Obesity, severe 2 | 2
Phenotype: Paroxysmal nonkines... 2 | 2
Phenotype: T-cell immunodefici... 2 | 2
Phenotype: Vitreoretinopathy, ... 2 | 2
Phenotype: {Alcohol dependence... 2 | 2
Phenotype: {Diabetes mellitus,... 2 | 2
Phenotype: {Nephrolithiasis, u... 2 | 2
Pick disease 2 | 2
Porphyria cutanea tarda, susce... 2 | 2
Porphyria variegata, susceptib... 2 | 2
Premature ovarian failure 11 2 | 2
Restrictive dermopathy, lethal 2 | 2
UV-sensitive syndrome 1 2 | 2
[Transferrin serum level QTL2] 2 | 2

This is where graphics are reside..
Name Gene Development Level Target Family Log Novelty  Pubmed Score  Antibody Count  Knowledge Availability 
Paired box protein Pax-3 PAX3 Tbio Transcription Factor -2.83871 692.1 400